Temple Syndrome: Comprehensive Clinical Study in Genetically Confirmed 60 Japanese Patients
These results clarify the detailed clinical characteristics of TS14. On the basis of these findings, we propose an efficient diagnostic approach and pertinent clinical management for TS14 patients.
Authors
- Masayo Kagami (ORCID: https://orcid.org/0000-0003-3020-455X)
- Tsutomu Ogata (ORCID: https://orcid.org/0000-0001-7178-9991)
- Hiromune Narusawa
- Yasuhiro Naiki (ORCID: https://orcid.org/0000-0002-6338-895X)
- Rika Kosaki (ORCID: https://orcid.org/0000-0002-4367-6129)
- Akie Nakamura
- Keiko Matsubara (ORCID: https://orcid.org/0000-0001-6254-9216)
- Keisuke Nagasaki (ORCID: https://orcid.org/0000-0002-5882-661X)
- Michihiko Aramaki (ORCID: https://orcid.org/0000-0001-7032-974X)
- Maki Fukami (ORCID: https://orcid.org/0000-0001-9971-4035)
- Tomoe Ogawa
Institutions
- Toho University (JP)
- Hamamatsu University (JP)
- Tohoku University (JP)
- Hamamatsu University School of Medicine (JP)
- Niigata University Medical and Dental Hospital (JP)
- National Center For Child Health and Development (JP)
- Hamamatsu Medical Center (JP)
- University of Yamanashi (JP)
- Niigata University (JP)
Publication Details
- Journal
- The Journal of Clinical Endocrinology & Metabolism
- Published
- 2024-12-18
- DOI
- https://doi.org/10.1210/clinem/dgae883
- Citations
- 6
- Primary Topic
- Genetic Syndromes and Imprinting
- Type
- article
- Field-Weighted Citation Impact
- 3.30
Funders
- National Center for Child Health and Development
- Japan Agency for Medical Research and Development
- Japan Society for the Promotion of Science